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Effect of Intensive Monitoring of Patients With Poorly Controlled Type 2 Diabetes With Different Glycemic Background

G

Goztepe Prof Dr Suleyman Yalcın City Hospital

Status

Completed

Conditions

Poor Glycemic Control
Type 2 Diabetes

Study type

Observational

Funder types

Other

Identifiers

NCT06385899
: Poorly controlled T2DM-12

Details and patient eligibility

About

In Turkey, only 55% of patients with type 2 diabetes have been diagnosed, and 91% of these patients have been receiving treatment. The rate of patients reaching the treatment target is 50%. The pandemic has also affected diabetic patients. It is aimed to determine the characteristics of patients with type 2 diabetes (HbA1c >=10) with poor metabolic control and to evaluate the extent to which metabolic control can be achieved in 12 months.

Full description

Patients who applied to Istanbul Medeniyet University Goztepe Prof. Dr. Suleyman Yalcin City Hospital Diabetes Polyclinics and have an HbA1c levels of >= 10% in their examinations will be admitted to the study. Detailed history, including medication usage and previous blood tests will be questioned. The patients will be asked to complete questionnaires about their eating patterns (mindful eating questionnaire), their physical activities (General practice physical activity questionnaire), and whether the participants have depression (Beck depression questionnaire). Anthropometric measurements will be taken, and biochemical data will be recorded. Patients will be grouped according to their previous HbA1c values as a) newly diagnosed, b) those whose diabetes was previously controlled, c) those whose diabetes was previously not at the target range but now worsened, and d) those whose diabetes was poorly controlled from the beginning. Diabetes follow-up will be continued by their respective physicians. The patients will be called again three months after their enrollment to record the most recent biochemical data. Patient characteristics (age, gender, educational status, depression status, eating awareness, exercise characteristics) will be evaluated in accordance with the predetermined HbA1c groups. Again, according to the patient groups, the difference in HbA1c after three months, the frequency of reaching the target, and possible factors associated with the findings will be evaluated.

Enrollment

266 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosed with type 2 diabetes
  • give consent to the study
  • accessibility to the previous and recent test results

Exclusion criteria

  • acute infection or inflammation lasting more than a week
  • acute metabolic decompensation
  • unable to attend to the follow-ups
  • having non-thyroid endocrine diseases
  • active oncologic treatment

Trial design

266 participants in 4 patient groups

Newly diagnosed diabetes
Description:
Patients who have been diagnosed with type 2 diabetes within a month
Had controlled diabetes before
Description:
Patients who had at least two HbA1c levels =\<%7,5 before enrollment
Had moderately uncontrolled diabetes
Description:
Patients who had at least two HbA1c levels between %7,5 and %9,49 before enrollment
Had poorly controlled diabetes
Description:
Patients who had at least two HbA1c levels above %9,5 before enrollment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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